Online Intervention for Reduction of Ultra-processed Products and Increase of Physical Activity i… (NCT05834842) | Clinical Trial Compass
UnknownNot Applicable
Online Intervention for Reduction of Ultra-processed Products and Increase of Physical Activity in University Students
176 participantsStarted 2024-09-01
Plain-language summary
This study evaluates the effectiveness of an online Multi-component psychological intervention, that is focused on reducing the consumption of ultra processed foods and increase the frequency of performing Physical Activity. At the same time to observe the effect on symptoms of anxiety, depression and stress.
Who can participate
Age range
18 Years – 35 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Have a device (cell phone, computer or tablet) with internet access.
* Have agreed to participate by giving tacit consent.
* Be enrolled in any degree from a university in Mexico
Exclusion Criteria:
* Be diagnosed with a psychiatric disorder.
* Being diagnosed with an eating disorder.
* Being under some nutritional food treatment.
* Have a physical disability or injury that prevents you from engaging in mild to moderate physical activity.
* Being under any pharmacological treatment for a medical condition.
* Leaving the instruments unfinished.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in the scores of the Frequency of Consumption
Timeframe: 1 to 1.5 months, depending on the development of the patient and the completion of the 9 modules
2
Change in time of the Physical Activity
Timeframe: 1 to 1.5 months, depending on the development of the patient and the completion of the 9 modules
3
Change in the Scale in Self- Efficacy Eating Consumption Scale (SEECS)
Timeframe: 1 to 1.5 months, depending on the development of the patient and the completion of the 9 modules
4
Change in the Self-Efficacy for Exercise Questionnaire (SEEQ)
Timeframe: 1 to 1.5 months, depending on the development of the patient and the completion of the 9 modules
5
Change in the Sedentary behavior questionnarie (SBQ-s)
Timeframe: 1 to 1.5 months, depending on the development of the patient and the completion of the 9 modules